abdominal surgery
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) patients over 40 years at the time of obtaining informed consent 2) of regular operation patients who undergo abdominal surgery under general anesthesia, those who are scheduled to be treated in the postoperative intensive care unit (ICU) 3) patients who have 3 hours or more of scheduled operation time 4) patients who have obtained consent from the person
Exclusion criteria
Exclusion criteria: 1) patients undergoing surgery requiring general anesthesia within 3 months prior to obtaining informed consent 2) patients with acute respiratory failure (pneumonia, acute respiratory distress syndrome etc.) 3) patients who undergo emergency surgery 4) patients with sepsis or septic shock 5) Patients with progressive neuromuscular disease 6) Patients undergoing thoracic surgery 7) highly obese patients (BMI 35 kg / m2 or more) 8) women who are pregnant or have pregnancy possibility 9) patients who received study drugs or investigational drugs within 3 months prior to obtaining informed consent 10) patinets whom research investigator has determined to be inappropriate
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| change in exhaled NO, NO2, HONO concentration during perioperative period | — |
Secondary
| Measure | Time frame |
|---|---|
| 1) relevance of exhaled NO, NO2, HONO and blood ROS during perioperative period 2) relevance of exhaled NO, NO2, HONO and blood cytokines during perioperative period 3) relevance of exhaled NO, NO2, HONO and blood biomarkers during perioperative period 4) relevance of exhaled NO, NO2, HONO and hematological examination, blood biochemical examination, arterial blood gas analysis examination during perioperative period 5) relevance of exhaled NO, NO2, HONO and pulmonary function during perioperative period 6) Whether the exhaled NO, NO2 and HONO concentrations are related to the anesthesia method during perioperative period 7) Whether the exhaled NO, NO 2 and HONO concentrations in the perioperative period are related to the operation conten | — |
Countries
Japan
Contacts
Tottori University Division of Anesthesiology and Critical Care Medicine